EP1811940A1 - Extrait de sophorae subsprostratae radix pour la prevention et le traitement de maladies respiratoires - Google Patents

Extrait de sophorae subsprostratae radix pour la prevention et le traitement de maladies respiratoires

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Publication number
EP1811940A1
EP1811940A1 EP05804515A EP05804515A EP1811940A1 EP 1811940 A1 EP1811940 A1 EP 1811940A1 EP 05804515 A EP05804515 A EP 05804515A EP 05804515 A EP05804515 A EP 05804515A EP 1811940 A1 EP1811940 A1 EP 1811940A1
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EP
European Patent Office
Prior art keywords
ova
sophorae radix
administration
airway
extract
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP05804515A
Other languages
German (de)
English (en)
Other versions
EP1811940A4 (fr
Inventor
Chang-Kyun Han
Kiwon Joung
Hunseung Yoo
Yong-Baik Cho
Keun Ho Ryu
Hye Yeon Baek
Taek-Soo Kim
In Ho Jung
Wie-Jong Kwak
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SK Chemicals Co Ltd
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SK Chemicals Co Ltd
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Publication of EP1811940A1 publication Critical patent/EP1811940A1/fr
Publication of EP1811940A4 publication Critical patent/EP1811940A4/fr
Withdrawn legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18—Magnoliophyta (angiosperms)
    • A61K36/185—Magnoliopsida (dicotyledons)
    • A61K36/48—Fabaceae or Leguminosae (Pea or Legume family); Caesalpiniaceae; Mimosaceae; Papilionaceae
    • A61K36/489—Sophora, e.g. necklacepod or mamani
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/02—Nasal agents, e.g. decongestants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2236/00—Isolation or extraction methods of medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicine
    • A61K2236/30—Extraction of the material
    • A61K2236/33—Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones

Definitions

  • This invention relates to Sophorae Radix extract useful for prevention and treatment of respiratory diseases.
  • This invention also relates to a pharmaceutical drug comprising Sophorae Radix extract useful for prevention and treatment of respiratory diseases due to their excellent effects in preventing airway contraction / respiratory infection, 5-lipoxygenase, phosphodiesterase 4, airway hyper- responsiveness or airway remodeling / leukotriene D4, as well as having an antitussive effect.
  • Asthma is a typical respiratory disease having repetitive and spasmodically symptoms of difficulty in breathing, coughs and stridor. About 30% pediatric asthma patients start to show the symptoms within one year from birth while about
  • Respiratory obstruction as one of characteristics of asthma occurs via 3 steps: i.e., contraction of bronchial smooth muscle, tylosis of pulmonary mucosa, and accumulation of sticky mucus in bronchi and bronchioles. Of them, contraction of bronchial smooth muscle is rather easily recovered.
  • IgE In the attack of extrinsic (allergic) asthma, it is known that IgE plays a very important role and IgG is also often involved. IgE releases mediators (histamine, SRS-A, ECF-A, NCF, PAF, Kinin, PGs, etc.) which induce a hypersensitivity reaction by activating mast cells. The cause of intrinsic (non-allergic) asthma is still not known but this kind of asthma appears to be mediated by autonomic nerves.
  • a cholinergic stimulus can directly release mediators such as histamine from mast cells, increase secretion of goblet cells, dilate pulmonary blood vessels, and contract trachea, bronchi, and large bronchioles, thereby causing bronchial spasm and increasing release of mucus.
  • asthma there is no cure for asthma. Although there are many methods and drugs which have been used for the prevention of spasm and complications due to asthma they have not been satisfactory. One of the most effective ways of preventing the attack of asthma may be to find the very factors that are involved in causing asthma. Examples of therapeutic agents that have been used to treat asthma are inhaling bronchodilator drugs, oral or injectable bronchodilator drugs (sympathetic stimulators and theophyllines), steroid preparations (inhaling, oral and injectable form, etc.), leukotriene antagonists (montelukast, pranlukast, zileuton, etc.), anti ⁇ allergic drugs ( cromolyn disodium, ketotifen, etc.) and the like.
  • bronchodilator drugs oral or injectable bronchodilator drugs (sympathetic stimulators and theophyllines), steroid preparations (inhaling, oral and injectable form, etc.), leukotriene antagonists (monteluka
  • Bronchitis can be either acute or chronic. According to its causes, bronchitis is divided into allergic, infectious, and extrinsic bronchitis, while pathologically it is classified catarrhalis, suppurative, occlusive, ulcerative, and infiltrative bronchitis. The most frequent cause of bronchitis is due to infection with bacteria, viruses, fungi and the like. People who normally not infected with the above pathogens can be infected when their systemic immune system gets weakened. Allergic bronchitis can be a direct allergic reaction due to inhalation of allergens or a partial symptom due to a generalized allergic reaction.
  • Extrinsic bronchitis may occur due to a chemical stimulus such as chlorine and sulfur dioxide gas, or due to a physical stimulus such as dusts.
  • a chemical stimulus such as chlorine and sulfur dioxide gas
  • a physical stimulus such as dusts.
  • People living in large cities with polluted air can be readily exposed to respiratory infections.
  • acute bronchitis from the pathological point of view, it is easy to observe ruber, swelling, and xerosis and also mucous or suppurative secretions.
  • asthmas can be recovered without incurring complications. However, if it is progressed into a chronic asthma, it results in swelling, tylosis and atrophy. In a prolonged chronic asthma, it results in fiber proliferation, bronchostenosis or pulmonary emphysema.
  • bronchitis The most peculiar symptoms of bronchitis are coughs and phlegm. If the cause of bronchitis is due to infection, there often develops fever and chest pain, whereas if it is due to extrinsic factors, there often develops irritations on the mucus of mouth, nose, eye, etc. In therapy, cough is considered as a sort of a bodily defense and thus it is not recommended to intentionally stop coughing. It is essential that a therapy for the cause be conducted along with other measures. In winter, it is desirable to increase room temperature and administer a small amount of codeine, atropine, ephedrine, antihistamine agents, and the like. Use of steroids or theophyllines for treating infections is not satisfactory.
  • Nasal allergic inflammation often refers to nasal allergy or allergic rhinitis. It entails symptoms of sudden, continuous coughs, release of a large amount of clear nasal . mucus, stuffy nose, heavy head, release of tears, and the like. When the symptoms are similar but the allergens are not identified it is coryza vasomotoria. For example, the above symptoms may occur when body temperature is temporarily lowered in the morning and they are usually recovered within a few hours, and these symptoms are commonly seen in people in a cold season. This can be sometimes confused with nasal cold but it differs from the cold and often accompanies asthma and hives.
  • the allergic reaction in allergic rhinitis is an antigen-antibody hypersensitivity reaction, wherein histamine is released from mast cells and cell walls of basophils, and arachidonic acid is released to produce prostaglandins and leukotrienes by cyclooxygenase (COX) and 5-li ⁇ ooxygenase(5-LO), thereby mediating the initial reaction occurring between 2 - 90 min after being exposed to an antigen and the post reaction occurring 4-8 hrs thereafter.
  • the initial reaction is proceeded with by a mediating substance while the post reaction is mediated by cell infiltration.
  • allergic and non-allergic rhinitis both serve as risk factors for developing asthma.
  • bronchodilator drugs such as anti-cholinergic drugs, beta 2 receptor agonist, etc.
  • bronchodilator drugs are not effective in treating inflammation but they simply alleviate the symptoms. Therefore, long-term use of the drugs may cause drug resistance and there is also a risk of exacerbation.
  • Steroids which are known effective in treating inflammation but they have serious side effects and are not suitable for long term use and also shown not effective in treating chronic bronchitis. Therefore, the above two drugs have been prescribed to be combined for administration but the steroids drug has been formulated in an inhalation form rather than as one for oral administration due to its adverse effects thus lowering its compliance due to the difficulty in administration.
  • respiratory diseases such as asthma, bronchitis, allergic rhinitis, acute lower respiratory infections(bronchitis, bronchiolitis, etc.), acute upper respiratory infection(tonsillitis, pharyngolaryngitis) but they are treated only for temporary release, and there is usually a problem of recurrence of the diseases after treatments. Therefore, prevention and treatment of respiratory diseases has been raised as one of the most important tasks to fulfill in medical science and the development of a novel therapeutic drug for the fundamental prevention and treatment of respiratory diseases is in urgent need.
  • Sophorae Radix of the present invention to be used as a crude drug is a shrub with a height of 1-2 m. It has about 2-5 cylindrical roots with yellowish brown color. Its stem has a cylindrical shape, has a groove on the surface and is densely covered with short and soft hairs where the upper part of the stem is normally bent in the form of " ⁇ .”, a Chinese letter. Its roots, which are used as drugs after drying, have a long cylindrical shape and are a bit bent with a length of 10-25-35 cm, a diameter of 0.3-1 cm. Its surface is brown or dark brown, has vertically-formed wrinkles and lengthy lenticels with a bit of rotation. Its main place of product is Gwangseozhou in China.
  • an object of the present invention is to provide a therapeutic drug for prevention and treatment of respiratory diseases comprising Sophorae Radix extract as an active ingredient.
  • Fig. 1 is a graph showing the effect on the airway hyper-responsiveness [SAL: saline, OVA: ovalbumin, SOS: extract prepared in Preparation Example 2];
  • Fig. 2 A-F are pictures showing the effect of the extract prepared in Preparation Example 2 (SOS) or montelukast on airway mucus expression in lung tissues of OVA-sensitized and -challenged mice;
  • Fig. 3 is a histogram showing the effect of the extract prepared in Preparation Example 2 (SOS) or montelukast on airway mucus expression in lung tissues of OVA-sensitized and -challenged mice;
  • Fig. 4 A-F are pictures showing the effect of the extract prepared in Preparation Example 2 (SOS) or montelukast on ⁇ -smooth muscle expression in lung tissues of OVA-sensitized and -challenged mice;
  • Fig. 5 is a histogram showing the effect of the extract prepared in Preparation Example 2 (SOS) or montelukast on ⁇ -smooth muscle expression in lung tissues of OVA-sensitized and -challenged mice;
  • Fig. 6 A-F are pictures showing the effect of the extract prepared in Preparation Example 2 (SOS) or montelukast on peribronchial fibrosis in lung tissues of OVA-sensitized and -challenged mice;
  • Fig. 7 is a histogram showing the effect of the extract prepared in Preparation Example 2 (SOS) or montelukast on fibrosis in lung tissues of OVA-sensitized and - challenged mice;
  • Fig. 8 is a histogram showing the effect of the extract prepared in Preparation
  • Fig. 9 is a result of Western blot showing the effect of the extract prepared in Preparation Example 2 (SOS) or montelukast on IL-4, IL-5, and IL-13 protein expression in lung tissues of OVA-sensitized and -challenged mice.
  • SOS Preparation Example 2
  • montelukast on IL-4, IL-5, and IL-13 protein expression in lung tissues of OVA-sensitized and -challenged mice.
  • the present invention relates to Sophorae Radix extract useful for prevention and treatment of respiratory diseases.
  • the present invention relates to a pharmaceutical drug comprising Sophorae Radix extract as an active ingredient which have excellent effects of inhibiting airway contraction, respiratory infections, 5-lipoxygenase activity, phosphodiesterase 4 activity, airway hyper-responsiveness, and inhibitory activity of airway remodeling; antagonistic activity against leukotriene D4; antitussive effect; therefore being useful for prevention and treatment of respiratory diseases such as asthma, acute and chronic bronchitis, allergic rhinitis, acute lower respiratory infection(bronchitis, bronchiolitis, etc.), acute upper respiratory infection(sphagitis, tonsillitis, laryngitis) and the like.
  • Crude Sophorae Radix is extracted via reflux by using about 7 to 10 times of water or an alcohol solution with reference to the weight of Sophorae Radix and then filtered.
  • the remnant is extracted again by adding about 4 to 7 times of water or an alcohol solution with reference to the weight of the combined Sophorae Radix, followed by heating, and then filtered.
  • two filtrates are combined together and filtered.
  • the above concentrate undergoes azeotropic concentration by adding about 20 to 50 times of water with reference to the total weight of the concentrate obtained in the above step 2), is uniformly suspended with an equal amount of water and is then placed under lyophilization. More specifically, the original crude Sophorae Radix is added with water or an alcohol solution and extracted under reflux for 2 to 5 hrs, wherein the amount of water or an alcohol solution is preferably about 7 to 10 times with reference to the weight of crude Sophorae Radix. Then, the above extract is filtered.
  • the filtrate is then added with about 4 to 7 times of water or an alcohol solution with reference to the weight of the crude Sophorae Radix, heated, reextracted for 2 - 5 lirs, filtered and combined with the previously obtained filtrate thereby increasing the extraction efficiency.
  • the extraction consists of the first extraction and the second extraction.
  • the present invention prevents the relatively low extraction efficiency obtained by the first extraction only.
  • a further study on the extraction efficiency by the inventors of the present invention showed about 80 - 90% of the total extract is obtained by the second extraction, which suggests that additional extractions of more than second extraction is not necessary and also uneconomical.
  • the extract obtained by the first and the second extractions as stated above is filtered, concentrated and then purified to get rid of unnecessary impurities such as proteins, polysaccharides, fatty acids and the like.
  • the filtrate is added with an equal amount of low grade alcohol or a nonpolar solvent to perform phase separation 2 - 4 times thereby obtaining solvent fraction while separating impurities.
  • low grade alcohols include alcohol having carbon atoms of from 1 to 6, preferably butyl alcohol, propyl alcohol, or isopropyl alcohol.
  • nonpolar solvents are ethylacetate, dichloromethane, chloroform, carbon tetrachloride or methylethylketone.
  • the fraction of a low grade alcohol or a nonpolar solvent obtained as a result of the above phase separation is concentrated under reduced pressure at 50 - 60 0 C to remove the solvent remaining in the specimen.
  • concentrated concentrate undergoes azeotropic concentration 2-3 times with about 25-50 times of water with reference to the total weight of the concentrate, and then uniformly suspended by adding an equal amount of water.
  • the extract of Sophorae Radix of the present invention can be obtained, in addition to the above-mentioned method, by extracting with water, water-saturated low grade alcohol or a nonpolar solvent followed by purification.
  • low grade alcohols include alcohol having carbon atoms of from 1 to 6, preferably butyl alcohol, propyl alcohol, or isopropyl alcohol.
  • nonpolar solvents are ethylacetate, dichloromethane, chloroform, carbon tetrachloride or methylethylketone.
  • Sophorae Radix extract undergoes lyophilization and then final extract is obtained in powder form.
  • This final extract has excellent activities of inhibiting airway contraction, respiratory inflammation, 5-lipoxygenase activity, phosphodiesterase 4 activity, airway hyper-responsiveness and airway remodeling; antagonistic activity against leukotriene D4, antitussive effect, etc., and is thus expected to be useful for the prevention and treatment of respiratory diseases.
  • the Sophorae Radix extract of the present invention can be administered in various oral and parenteral forms during clinical studies. When they are formulated diluents such as a filler, a bulking agent, a binder, a wetting agent, a disintegrating agent, a surfactant and the like or an excipient are used.
  • diluents such as a filler, a bulking agent, a binder, a wetting agent, a disintegrating agent, a surfactant and the like or an excipient are used.
  • Solid preparations for oral administration include tablets, pills, powders, granules, capsules, troches, suppositories and the like. These solid preparations are prepared by adding at least one excipient selected from the group consisting of starch, calcium carbonate, sucrose or lactose, gelatin, and the like to a mixture of lignan and lactone compound or its derivative. Besides, in addition to a simple excipient, a lubricant such as magnesium stearate, talc, and the like can be used.
  • Bases for suppositories are hard fat triglyceride esters, polyethylene glycol, polysorbate, cacao oil, laurin butter, glycerol, gelatin and the like.
  • Liquid preparations for oral administration are suspensions, solutions (syrups, drinks, etc.), emulsion and the like.
  • various excipients such as wetting agents, sweeteners, flavoring agents, and preservatives can be used in addition to the most frequently used diluents such as water and liquid paraffin.
  • Preparations for parenteral administration are sterilized solutions, non ⁇ aqueous solutions, suspensions, emulsions, lyophilizers.
  • Solvents for non-aqueous solutions, suspensions or emulsions are vegetable oils, propylene glycol, polyethylene glycol, olive oil, and ethyl oleate.
  • Sophorae Radix extract of the present invention has been used in folk remedies for long time and its safety has been confirmed by toxicity test. The dosage of the Sophorae Radix extract depends on various factors such as the rate of body absorption, body weight, age, sex, health conditions, diets of a subject and time required for administration, method of administration, excretion rate, seriousness of diseases, and the like.
  • Sophorae Radix extract As shown in pharmacological experiments, it is preferable to administer Sophorae Radix extract about 1-15 mg/kg of body weight. Therefore, the Sophorae Radix extract of the present invention to be used as an active ingredient of a pharmaceutical drug should be manufactured considering the effective range of pharmaceutical efficacies, and thus manufactured pharmaceutical preparations in the form of unit formulation can be administered at regular intervals and/ or according to a specialized medication committed under the supervision of a medical specialist or by the request of a subject.
  • Preparation Example 1 Preparation of Sophorae Radix extract 25Og of Sophorae Radix minced to a size of about 1.0 cm were well mixed and added with 2 L of water and then heat-extracted for 5 hrs while stirring. The resulting filtrate was collected and the remnant was added with 1.5 L of water and heat-extracted for 3 hrs. The above two filtrates were combined and then concentrated to the final volume of 1.5 L. The above concentrate was added with an equal volume of water-saturated n-butyl alcohol and performed phase separation 3 times. Only n-butyl alcohol fraction was collected and concentrated under reduced pressure at 58 0 C until the extract becomes dry.
  • Sophorae Radix was cleaned with water and dried. 25Og of the Sophorae Radix was added with 2 L of 50%(v/v) ethanol solution and extracted under reflux for 6 hrs while stirring. The resulting filtrate was collected and the remnant was added with 1.5 L of 30%(v/v) ethanol solution and heat-extracted for 3 hrs. The above two filtrates were combined and then concentrated to the final volume of 1.5 L.
  • the above concentrate was added with an equal volume of water-saturated n-butyl alcohol and performed phase separation 3 times. Only n-butyl alcohol fraction was collected and concentrated under reduced pressure at 58 0 C until the extract becomes dry. After most of the n-butyl alcohol and water are evaporated, it was added with 0.2 L of water and performed azeotropic concentration 3 times. The resultant was resuspended in an equal volume of distilled water and then lysophilized to finally obtain Sophorae Radix extract in powder.
  • Sophorae Radix was cleaned with water and dried. 25Og of the Sophorae
  • a Hartely male guinea pig(400 - 450 g, SLC, Japan) was sensitized by intravenously injecting 1.5 mL/kg of anti-ovalbumin anti-serum. 48 hrs after the sensitization, the guinea pig was administered with a drug orally. In 30 min, the guinea pig was pretreated by injecting 10 mg/kg of pyrilamine maleate, 10 mg/kg of indomethacin, and 0.1 mg/kg of propranolol subcutaneously, respectively. Then, the guinea pig was placed in Double Chamber Plethysmograph Box(HSE, Germany) installed with plethysmometer for measuring various respiratory indices and measured basic airway resistance values. 30 min after the pretreatment, 1% OVA was nebulized for 2 min in the form of aerosol by preparing a compressed air under high pressure. Airway resistance was measured for 30 min as an indicator of bronchospasm. Table 2
  • the Sophorae Radix extract of the present invention has an effect of inhibiting airway contraction in a sensitized guinea pig.
  • a 6 week old BALB/ c female mouse (SLC, Japan) was sensitized by administering 0.2 mL of a mixture consisting of 10 ⁇ g of OVA and alum intraperitoneally at Days 0, 7 and 14, respectively. 8 and 10 days after the last sensitization, 0.7% OVA was sprayed to the mouse for 50 min in the form of aerosol by a compressed air under high pressure to induce airway inflammation. 24 hrs after the induction of the airway inflammation, the bronchialveolar were washed with 1.5 mL of a phosphate buffer solution. The washed solution was collected and the number of leukocytes and eosinophils in the washed solution were counted, respectively.
  • the Sophorae Radix extract of the present invention has an effect of inhibiting airway infection. While the effect of montelukast as a positive control exhibits saturation of pharmaceutical efficacy at a relatively low level without dosage-dependent effect, the Sophorae Radix extract of the present invention is shown to have sufficient pharmaceutical effect which is also dosage-dependent.
  • PBML Human peripheral blood mononulear leukocyte
  • HBSS Hank's balanced salt solution
  • Sophorae Radix extract was added to the above mixture
  • arachidonic acid was added as a base material and produced leukotriene B4 (LTB4) for 15 min.
  • LTB4 leukotriene B4
  • Sophorae Radix extract of the present invention has an effect of inhibiting 5-lipoxygenase activity.
  • Example 5 Inhibition of Phosphodiesterase 4 (PDE4) Activity
  • PDE4 Phosphodiesterase 4
  • Example 6 Antagonistic Activity against Leukotriene D4 Receptor (LTD4)
  • LTD4 Leukotriene D4 Receptor
  • LTD4 receptor isolated from the pulmonary tissues of a Duncan Hartely guinea pig was stabilized in 50 mM Tris-HCl buffer solution (5 mM CaCb, 5 mM MgCk, 100 ⁇ g/mL bacitracin, 1 mM benzamidine, 0.1 mM phenylmethylsulfonyl fluoride) at 25 °C. Then, Sophorae Radix extract and 0.2 nM [3H]LTD4 were added to the above mixture and allowed to react. Binding rate was analyzed via Radioligand binding assay, and non-specific binding was determined by means of 0.1 ⁇ M LTD4. Specific binding rate 85%, Kd 0.2 nM, Bmax 0.24 pmol/mg protein. Table 6
  • the method used was the method by M.H. Boskabady et al. (Journal of Entnopharmacology 97, 2005, 79-82) with a bit of modifications.
  • a Hartley male guinea pig (450 ⁇ 500 g, SLC, Japan) was orally administered with a drug. 1 hr after the administration, the guinea pig was placed in Double Chamber Plethysmograph Box (HSE, Germany) installed with plethysmometer and stabilized by allowing a 5 min of time for adaptation. After the stabilization, 0.6M citric acid was sprayed to the guinea pig for 7 min in the form of aerosol by preparing a compressed air under high pressure. The guinea pig was observed continuously by a trained observer and the number of coughs induced by the above spray of citric acid aerosol was measured by using a microphone and a speaker. The coughs were distinguished from a normal sneeze due to its particular signs such as a peculiar and high sound with its mouth open, movement of abdomen, and an instant change in air flow. Table 7
  • Example 8 Inhibition of Airway Hyper-responsiveness
  • Six week old female BALB/ c mice (SLQ Japan) were sensitized by administering 0.2 mL of a mixture consisting of 10 ⁇ g of OVA and alum intraperitoneally at Days 0, 7 and 14, respectively.
  • OVA 0.7% OVA was sprayed to the mice for 50 min in the form of aerosol by preparing a compressed air under high pressure to induce airway hyper-responsiveness.
  • the measurement of airway hyper-responsiveness was conducted in a barometric plethysmography chamber (All Medicus, Seoul, Korea) while allowing all the mice in the chamber free movements and with consciousnesss.
  • Example 9 Inhibition of Airway Remodeling Eight to ten week old aseptically treated female BALB /c mice were sensitized by intraperitoneally injecting at Day 1 a mixed solution consisting of 500 ⁇ g of OVA and 1.0 mg of aluminum hydroxide (first treatment), and then inhaled with 2% OVA at Day 11 using an ultrasonic sprayer (second treatment), and finally inhaled with 3% OVA at Days 21, 22 and 23 (third treatment). The mice were then allowed to inhale 1% OVA for the following 6 weeks at intervals of 3 days and constructed an asthma model with induced airway remodeling. In the evening 24 hr prior to the 3rd OVA inhalation, the mice were administered once with the extract (SOS) prepared in Preparation Example 2.
  • SOS extract
  • mice were administered twice daily with the extract (SOS) prepared in Preparation Example 2 at the 3 rd OVA inhalation day (Day 21, 22, and 23), i.e., one administration at 1 hr prior to the inhalation and the other administration in the evening of the 3 rd OVA inhalation day.
  • SOS extract prepared in Preparation Example 2
  • the mice were administered twice daily.
  • the following assays were used for the analysis of the airway remodeling.
  • Collagen assay Method for quantitative analysis of the level of tissue fibrosis
  • ⁇ Peribronchial trichrome stain Method of identifying the level of fibrosis at the lower bronchus of peribronchial area by staining tissues using Masson's trichrome. All bronchi are similar in size based on the length of the basal membrane and thus 10 bronchi with circular shape are selected and their average value is obtained. The thickness of basal membrane based on bronchioles having an internal diameter of 150-200 ⁇ m are indicated in ⁇ m and the ratio is measured by using a computerized image analyzer program.
  • Fig. 2 shows the effect of the extract prepared in Preparation Example 2 (SOS) or montelukast on airway mucus expression in lung tissues of OVA-sensitized and - challenged mice. Representative PAS-stained sections of the lungs.
  • SOS Preparation Example 2
  • montelukast montelukast
  • the percentage of airway epithelium staining positively with PAS was increased significantly at 48 hrs after OVA inhalation compared to the percentage after saline inhalation (Figs. 2 and 3).
  • the increased percentage of airway epithelium staining positively with PAS was significantly reduced by the administration of SOS or montelukast.
  • Fig. 4 shows the effect of the extract prepared in Preparation Example 2 (SOS) or montelukast on ⁇ -smooth muscle expression in lung tissues of OVA-sensitized and -challenged mice. Representative immunohistochemical-stained sections for ⁇ - smooth muscle actin of the lungs.
  • Sampling was performed at 48 hrs after the last challenge in saline-inhaled mice with the administration of saline (A), OVA-inhaled mice with the administration of saline (B), OVA-inhaled mice with the administration of montelukast (C), OVA-inhaled mice with the administration of SOS 50mg/kg (D), OVA-inhaled mice with the administration of SOS 100mg/kg (E), and OVA-inhaled mice with the administration of SOS 200mg/kg (F). Bars indicate scale of 50 ⁇ m. Bars indicate scale of 50 ⁇ m. Bars indicate scale of 50 ⁇ m. Bars indicate scale of 50 ⁇ m.
  • Fig. 5 shows the effect of the extract prepared in Preparation Example 2 (SOS) or montelukast on ⁇ -smooth muscle expression in lung tissues of OVA-sensitized and -challenged mice.
  • SOS Preparation Example 2
  • montelukast OVA-inhaled mice with the administration of montelukast
  • Fig. 6 shows the effect of the extract prepared in Preparation Example 2 (SOS) or montelukast on peribronchial fibrosis in lung tissues of OVA-sensitized and - challenged mice.
  • FIG. 7 shows the effect of the extract prepared in Preparation Example 2 (SOS) or montelukast on fibrosis in lung tissues of OVA-sensitized and -challenged mice.
  • SOS Preparation Example 2
  • the area of peribronchial trichrome staining in paraffin-embedded lung was measured at 48 hrs after the last challenge in saline-inhaled mice with the administration of saline (SAL+SAL), OVA-inhaled mice with the administration of saline (OVA+SAL), OVA-inhaled mice with the administration of montelukast (OVA+MONTE), OVA-inhaled mice with the administration of SOS 50mg/kg (OVA+SOS50), OVA-inhaled mice with the administration of SOS 100mg/kg (OVA+SOS100), and OVA-inhaled mice with the administration of SOS 200mg/kg (OVA+SOS200). Bars represent mean SEM
  • the area of peribronchial trichrome staining was increased significantly at 48 hrs after OVA inhalation compared to the area after saline inhalation (Figs. 6 and 7).
  • the increased area of of peribronchial trichrome staining was significantly reduced by the administration of SOS or montelukast.
  • Fig. 8 shows the effect of the extract prepared in Preparation Example 2 (SOS) or montelukast on total lung collagen content of OVA-sensitized and -challenged mice.
  • SOS Preparation Example 2
  • montelukast The amount oflung collagen was measured using a collagen assay kit.
  • the levels of lung collagen were increased significantly at 48 hrs after OVA inhalation compared to the area after saline inhalation (Fig. 8). The increased levels of lung collagen were significantly reduced by the administration of SOS or montelukast.
  • cytokines IL-4, 5 and 13
  • concentration of OVA-specific IgE in the serum were measured by using ELISA kit(cytokine: R&D systems, Abingdon, UK/ OVA-specific IgE; BD sciences).
  • Fig. 9 shows the effect of the extract prepared in Preparation Example 2 (SOS) or montelukast on IL-4, IL-5, and IL-13 protein expression in lung tissues of OVA- sensitized and -challenged mice.
  • SOS Preparation Example 2
  • montelukast montelukast on IL-4, IL-5, and IL-13 protein expression in lung tissues of OVA- sensitized and -challenged mice.
  • IL-4, IL-5, and IL-13 protein expression were measured at 48 hrs after the last challenge in saline-inhaled mice with the administration of saline (SAL+SAL), OVA-inhaled mice with the administration of saline (OVA+SAL), OVA-inhaled mice with the administration of montelukast (OVA+ MONTE), OVA-inhaled mice with the administration of SOS 50mg/kg (OVA+SOS50), OVA-inhaled mice with the administration of SOS 100mg/kg (OVA+SOS100), and OVA-inhaled mice with the administration of SOS 200mg/kg (OVA+SOS200). Results were similar in 8 independent experiments.
  • Sophorae Radix extract prepared in Preparation Examples 1 - 3 were suspended and administered orally in the amount of 2 g/kg for a period of 2 weeks to rats. Each group contained six animals.
  • mice After the administration, the mice were observed with respect to their death, clinical symptoms, change in body weight, hematological and hematobiochemical tests were performed. The mice were then autopsied to examine any abnormalties in their abdominal and pectoral organs with naked eyes. The results showed that all the mice survived and there were no particular signs in terms of clinical symptoms. Further, there were no significant findings in toxicity test in hematological and hematobiochemical tests as well as in autopsies. Therefore, it was confirmed that the Sophorae Radix extract of the present invention is a safe material which does not exhibit any toxicity in rats up to the dosage of 2,000 mg/kg.
  • Sophorae Radix extract of the present invention with the following composition was formulated in tablets for oral administration by using wet granulation and dry granulation methods.
  • Sophorae Radix extract 250 mg, light anhydrous silicone dioxide 10 mg, magnesium stearate 2 mg, microcrystalline cellulose 50 mg, sodium starch glycolate 25 mg, corn starch 113 mg, adequate amount of anhydrous ethanol.
  • Formulation Example 2 Preparation of Ointments Sophorae Radix extract of the present invention with the following composition was formulated in ointments.
  • composition 1 Sophorae Radix extract of the present invention with the following compositions was formulated in topical agents.
  • Sophorae Radix extract 0.3 g, sodium polyacrylate 1.3 g, glycerine 3.6 g, hydroxy aluminum 0.04 g, methyl parabene 0.2 g, water 14 g.
  • composition 2 Sophorae Radix extract 0.6 g, propylene glycol 1.6 g, liquid paraffin 0.8 g, isopropyl myristate 0.4 g, acrylic adhesive 143Og, water 16.4 g.
  • Sophorae Radix extract of the present invention with the following composition was formulated in troches. [Composition]
  • Sophorae Radix extract of the present invention with the following composition was formulated in syrups.
  • Composition Sophorae Radix extract 2 g, saccharin 0.8 g, sugar 25.4 g, glycerine 8.O g, flavor 0.04 g, ethanol 4.0 g, sorbic acid 0.4 g, adequate amount of distilled water
  • the Sophorae Radix extract of the present invention unlike the conventional synthesized pharmaceutical drugs which have shown effective only in limited cases of respiratory diseases model, have exhibited excellent pharmaceutical efficacies in overall respiratory diseases model. That is, the
  • Sophorae Radix extract of the present invention has excellent effect of inhibiting airway contraction, respiratory infections, 5-lipoxygenase activity, phosphodiesterase 4 activity, airway hyper-responsiveness and airway remodeling; antagonistic activity against leukotriene D4; and antitussive effect, thus being useful for prevention and treatment of respiratory diseases, such as asthma, acute and chronic bronchitis, allergic rhinitis, acute lower respiratory infections (bronchitis, bronchiolitis, etc.), acute upper respiratory infections (sphagitis, tonsillitis, laryngitis).
  • respiratory diseases such as asthma, acute and chronic bronchitis, allergic rhinitis, acute lower respiratory infections (bronchitis, bronchiolitis, etc.), acute upper respiratory infections (sphagitis, tonsillitis, laryngitis).

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Abstract

La présente invention se rapporte à un extrait isolé de Sophorae subprostratae Radix utile pour la prévention et le traitement de maladies respiratoires. Plus spécifiquement, la présente invention se rapporte à un médicament pharmaceutique comprenant l'extrait de Sophorae subprostratae Radix et présentant d'excellents effets d'inhibition de la contraction des voies aériennes, des infections respiratoires, de l'activité 5-lipoxygénase, de l'activité phosphodiestérase 4, de l'hyperréactivité des voies aériennes et du remodelage des voies aériennes; de l'activité antagoniste dirigée contre du leucotriène D4; ainsi qu'un effet antitussif, ledit médicament s'avérant par conséquent utile pour la prévention et le traitement des maladies respiratoires telles que l'asthme, la bronchite aiguë ou chronique, la rhinite allergique, les infections respiratoires supérieures aiguës et les infections respiratoires inférieures aiguës, et analogues.
EP05804515A 2004-10-27 2005-10-21 Extrait de sophorae subsprostratae radix pour la prevention et le traitement de maladies respiratoires Withdrawn EP1811940A4 (fr)

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PCT/KR2005/003522 WO2006046814A1 (fr) 2004-10-27 2005-10-21 Extrait de sophorae subsprostratae radix pour la prevention et le traitement de maladies respiratoires

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KR101086037B1 (ko) 2011-11-22
US9180153B2 (en) 2015-11-10
RU2007118579A (ru) 2008-12-10
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US20100221371A1 (en) 2010-09-02
RU2390349C2 (ru) 2010-05-27
CA2585657A1 (fr) 2006-05-04
EP1811940A4 (fr) 2009-12-02
JP5384828B2 (ja) 2014-01-08
AU2005300218A1 (en) 2006-05-04
CN103690594A (zh) 2014-04-02

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